{"title":"成功分阶段的手术治疗闭锁与尿道直肠瘘的雄性小猫。","authors":"Nithida Boonwittaya, Wutti Bunjerdsuwan, Piyathip Choochalermporn","doi":"10.1177/20551169251337835","DOIUrl":null,"url":null,"abstract":"<p><strong>Case summary: </strong>A 2-month-old male British Shorthair cat was referred with suspected atresia ani. Physical examination revealed an imperforate anus and dribbling of faecal discharge through the penis. Radiographic findings, along with a retrograde urethrogram, confirmed the diagnosis of type II atresia ani with a urethrorectal fistula. Surgical anoplasty was performed and the patient recovered well. At 8 months of age, surgical treatment for the congenital urethrorectal fistula was carried out via a single perineal approach, including fistulectomy and castration through the same incision. Postoperative short-term outcomes were excellent, with normal defecation and urination.</p><p><strong>Relevance and novel information: </strong>Atresia ani is a rare congenital anomaly, particularly in male cats. Despite advancements in surgical techniques, this case represents the first successful staged surgical management of urethrorectal fistula with type II atresia ani in a male kitten, potentially influencing future surgical approaches for similar congenital anomalies.</p>","PeriodicalId":36588,"journal":{"name":"Journal of Feline Medicine and Surgery Open Reports","volume":"11 1","pages":"20551169251337835"},"PeriodicalIF":0.7000,"publicationDate":"2025-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12144339/pdf/","citationCount":"0","resultStr":"{\"title\":\"Successful staged surgical management of atresia ani with urethrorectal fistula in a male kitten.\",\"authors\":\"Nithida Boonwittaya, Wutti Bunjerdsuwan, Piyathip Choochalermporn\",\"doi\":\"10.1177/20551169251337835\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Case summary: </strong>A 2-month-old male British Shorthair cat was referred with suspected atresia ani. Physical examination revealed an imperforate anus and dribbling of faecal discharge through the penis. Radiographic findings, along with a retrograde urethrogram, confirmed the diagnosis of type II atresia ani with a urethrorectal fistula. Surgical anoplasty was performed and the patient recovered well. At 8 months of age, surgical treatment for the congenital urethrorectal fistula was carried out via a single perineal approach, including fistulectomy and castration through the same incision. Postoperative short-term outcomes were excellent, with normal defecation and urination.</p><p><strong>Relevance and novel information: </strong>Atresia ani is a rare congenital anomaly, particularly in male cats. Despite advancements in surgical techniques, this case represents the first successful staged surgical management of urethrorectal fistula with type II atresia ani in a male kitten, potentially influencing future surgical approaches for similar congenital anomalies.</p>\",\"PeriodicalId\":36588,\"journal\":{\"name\":\"Journal of Feline Medicine and Surgery Open Reports\",\"volume\":\"11 1\",\"pages\":\"20551169251337835\"},\"PeriodicalIF\":0.7000,\"publicationDate\":\"2025-06-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12144339/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Feline Medicine and Surgery Open Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1177/20551169251337835\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"VETERINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Feline Medicine and Surgery Open Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/20551169251337835","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"VETERINARY SCIENCES","Score":null,"Total":0}
Successful staged surgical management of atresia ani with urethrorectal fistula in a male kitten.
Case summary: A 2-month-old male British Shorthair cat was referred with suspected atresia ani. Physical examination revealed an imperforate anus and dribbling of faecal discharge through the penis. Radiographic findings, along with a retrograde urethrogram, confirmed the diagnosis of type II atresia ani with a urethrorectal fistula. Surgical anoplasty was performed and the patient recovered well. At 8 months of age, surgical treatment for the congenital urethrorectal fistula was carried out via a single perineal approach, including fistulectomy and castration through the same incision. Postoperative short-term outcomes were excellent, with normal defecation and urination.
Relevance and novel information: Atresia ani is a rare congenital anomaly, particularly in male cats. Despite advancements in surgical techniques, this case represents the first successful staged surgical management of urethrorectal fistula with type II atresia ani in a male kitten, potentially influencing future surgical approaches for similar congenital anomalies.